3206-31-3 Usage
General Description
Triethyl nitrilotricarboxylate is a chelating agent commonly used in chemical and industrial applications. It is a clear, colorless liquid with a slight ammonia-like odor and is soluble in water. This chemical is widely used in the formulation of metal cleaning products, metal plating solutions, and as a corrosion inhibitor in industrial water treatment. Triethyl nitrilotricarboxylate is known for its ability to bind to metal ions, preventing them from precipitating or forming unwanted deposits. Additionally, it is used in the production of pharmaceuticals and as a complexing agent in analytical chemistry. Overall, it is an important chemical that plays a critical role in various industrial and scientific processes.
Check Digit Verification of cas no
The CAS Registry Mumber 3206-31-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,0 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3206-31:
(6*3)+(5*2)+(4*0)+(3*6)+(2*3)+(1*1)=53
53 % 10 = 3
So 3206-31-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO6/c1-4-14-7(11)10(8(12)15-5-2)9(13)16-6-3/h4-6H2,1-3H3
3206-31-3Relevant articles and documents
Heterocyclic Polyfluoro-compounds. Part 40. Preparation of Polyfluoroazepines
Barlow, Michael G.,Harrison, Geoffrey M.,Haszeldine, Robert N.,Morton, William D.,Shaw-Luckman, Peter,Ward, Mavis D.
, p. 2101 - 2104 (2007/10/02)
The hexafluoro-Dewar-benzene adduct of phenyl azide yields hexafluoro-1-phenyl-1H-azepine on pyrolysis.Reaction of ethyl azidoformate with hexafluorobenzene yields ethyl hexafluoro-1H-azepine-1-carboxylate (21percent), with octafluoronaphthalene yields 1,2-(ethoxycarbonylimino)-1,2,3,4,5,6,7,8-octafluoro-1,2-dihydronaphthalene (23percent), and with 1,2,3,4-tetrafluoronaphthalene yields 1,2-(ethoxycarbonylimino)-1,2,3,4-tetrafluoro-1-12-dihydronaphthalene (18percent) and ethyl 5,6,7,8-tetrafluoro-1-naphthylcarbamate (48percent).No azepines were obtained from the reaction of cyanogen azide with the two naphthalenes.
